Synergistic Coupling of Proton Conductors BaZr0.1Ce0.7Y0.1Yb0.1O3-δ and La2Ce2O7 to Create Chemical Stable, Interface Active Electrolyte for Steam Electrolysis Cells

被引:62
|
作者
Li, Wenyuan [1 ]
Guan, Bo [1 ]
Ma, Liang [1 ,2 ]
Tian, Hanchen [1 ]
Liu, Xingbo [1 ]
机构
[1] West Virginia Univ, Benjamin M Statler Coll Engn & Mineral Resources, Mech & Aerosp Engn Dept, Morgantown, WV 26506 USA
[2] Hebei Univ Engn, Sch Mat Sci & Engn, Handan 056038, Peoples R China
关键词
steam electrolysis; proton conductors; triple-conducting; BZCYYb stability; La2Ce2O7; barrier layer; OXIDE FUEL-CELLS; OXYGEN-ION; TEMPERATURE; TRANSPORT; PERFORMANCE; ANODE; REVERSIBILITY; STABILITY; EFFICIENT; BEHAVIOR;
D O I
10.1021/acsami.9b00303
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
For the first time, proton conductors BaZr0.1Ce0.7Y0.1Yb0.1O3-delta (BZCYYb) and La2Ce2O7 (LCO) are combined to create an interface active and steam-tolerant electrolyte for high-performance proton-conducting solid oxide electrolysis cells. LCO shows good chemical compatibility with BZCYYb. The readily fabricated LCO/BZCYYb bilayer electrolyte can be densified at a temperature of as low as 1300 degrees C versus similar to 1600 degrees C for the benchmark steam-stable BaZr0.8Y0.2O3-delta electrolyte. With Pr2NiO4+delta as the anode and Ni as the cathode catalyst, this bilayer electrolyte cell yields a current density of 975 and 300 mA/cm(2) under a 1.3 V applied potential at 700 and 600 degrees C, respectively. This performance is among the best of all H-SOECs equipped with a chemically stable electrolyte so far. A BZCYYb layer in the bilayer electrolyte promotes the hydrogen evolution reaction at the cathode side, resulting in a 108% improvement over the cell without this layer. The LCO layer, on the other hand, effectively protects this functional BZCYYb layer from the high concentration of steam in a practical SOEC operation condition. The cell without the LCO layer shows degradation in terms of an increased electrolyzing potential from 1.07 to 1.29 V during a constant 400 mA/cm(2) operation at 700 degrees C. In contrast, the bilayer electrolyte cell maintains the same electrolyzing potential of 1.13 V under the same conduction for a 102 h operation. These findings demonstrate that this synergic bilayer electrolyte design is a vital strategy to overcome the dilemma between performance and stability faced by the current benchmark Zr- or Ce-rich Ba(CeZr)O3-delta electrolysis cells to achieve excellent performance and stability at the same time.
引用
收藏
页码:18323 / 18330
页数:8
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